Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C10H16O |
| Molecular Weight | 152.2334 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=C)[C@@H]1CC=C(C)[C@H](O)C1
InChI
InChIKey=BAVONGHXFVOKBV-NXEZZACHSA-N
InChI=1S/C10H16O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9-11H,1,5-6H2,2-3H3/t9-,10-/m1/s1
| Molecular Formula | C10H16O |
| Molecular Weight | 152.2334 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Cloning and expression of a rat liver phenobarbital-inducible UDP-glucuronosyltransferase (2B12) with specificity for monoterpenoid alcohols. | 1995 Oct 1 |
|
| Degradation of pinene by Bacillus pallidus BR425. | 1998 |
|
| Species differences in the metabolism of (+)- and (-)-limonenes and their metabolites, carveols and carvones, by cytochrome P450 enzymes in liver microsomes of mice, rats, guinea pigs, rabbits, dogs, monkeys, and humans. | 2002 |
|
| Effects of Anethum graveolens L. seed extracts on experimental gastric irritation models in mice. | 2002 Dec 19 |
|
| Metabolism of (+)- and (-)-limonenes to respective carveols and perillyl alcohols by CYP2C9 and CYP2C19 in human liver microsomes. | 2002 May |
|
| Monoterpene biosynthesis pathway construction in Escherichia coli. | 2003 Sep |
|
| Cell adaptation to solvent, substrate and product: a successful strategy to overcome product inhibition in a bioconversion system. | 2005 Dec |
|
| Adaptation of Rhodococcus erythropolis DCL14 to growth on n-alkanes, alcohols and terpenes. | 2005 May |
|
| Herbal monoterpene alcohols inhibit propofol metabolism and prolong anesthesia time. | 2006 May 30 |
|
| Monoterpenoid agonists of TRPV3. | 2007 Jun |
|
| Inhibitory effects of substrate and product on the carvone biotransformation activity of Rhodococcus erythropolis. | 2008 Jul |
|
| Distinct effects of carvone analogues on the isolated nerve of rats. | 2010 Oct 25 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:52:51 GMT 2023
by
admin
on
Fri Dec 15 16:52:51 GMT 2023
|
| Record UNII |
OOZ105PLI9
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
DTXSID701036409
Created by
admin on Fri Dec 15 16:52:51 GMT 2023 , Edited by admin on Fri Dec 15 16:52:51 GMT 2023
|
PRIMARY | |||
|
2102-59-2
Created by
admin on Fri Dec 15 16:52:51 GMT 2023 , Edited by admin on Fri Dec 15 16:52:51 GMT 2023
|
PRIMARY | |||
|
330573
Created by
admin on Fri Dec 15 16:52:51 GMT 2023 , Edited by admin on Fri Dec 15 16:52:51 GMT 2023
|
PRIMARY | |||
|
218-270-5
Created by
admin on Fri Dec 15 16:52:51 GMT 2023 , Edited by admin on Fri Dec 15 16:52:51 GMT 2023
|
PRIMARY | |||
|
OOZ105PLI9
Created by
admin on Fri Dec 15 16:52:51 GMT 2023 , Edited by admin on Fri Dec 15 16:52:51 GMT 2023
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
RACEMATE -> ENANTIOMER |
